JOB DESCRIPTION

Are you passionate about ensuring the highest standards in GMP compliance and validation processes? Do you thrive on working in a dynamic, collaborative environment where your expertise makes a real difference? If so, we have the perfect opportunity for you.
As the Validation Lead, you will be the technical expert for validation at the ADM Denmark site. You’ll play a key role in implementing the site validation strategy, ensuring that our products are manufactured using equipment, facilities, and processes that meet GMP requirements as defined by the company and regulatory bodies.
Key Responsibilities:

Validation Strategy:

• Support the Validation Manager H&W Europe in executing the site validation strategy in line with the Site Validation Master Plan and regulatory requirements (ISO, GMP, etc.).
• Assist in implementing and maintaining the Validation QMS at the ADM Denmark site.
• Ensure project work is planned, executed, and completed efficiently and on time.
• Monitor validation schedules to ensure routine validation activities are completed as planned.

Validation Documentation & Risk Assessments:

• Develop, review, and execute validation protocols, plans, and reports to ensure compliance with regulatory standards.
• Conduct risk assessments for validation activities and develop mitigation plans to address any potential risks.

Validation Technical Expertise:

• Provide technical expertise and execute Equipment, Computer Systems, Process, and Cleaning Validation as needed.
• Participate in internal and external audits as required.
• Attend change control meetings and assess validation impacts.

What We’re Looking For:

• Strong understanding of GMP and validation principles.
• Excellent numeracy, analytical, and IT literacy skills.
• Strong communication and relationship-building abilities.
• Proven ability to manage multiple projects independently and collaboratively.
• Degree in a scientific or engineering field (or equivalent experience).
• Knowledge of GMP within the pharmaceutical industry.
• Familiarity with validation requirements in the pharmaceutical sector.

Why Join ADM?
Be part of a leading global organization committed to excellence and innovation.
Work in a collaborative, inclusive, and dynamic environment.
Take on a role where your expertise and input will shape the future of validation processes at ADM Denmark.
If you’re ready to take your career to the next level and make an impact, we’d love to hear from you.
Apply Now and become part of a team dedicated to delivering excellence in every product we manufacture.

Please refer the Job description for details